{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Lawrence",
      "address_1": "350 Merrimack Street",
      "reason_for_recall": "Product may be mislabeled.",
      "address_2": "",
      "product_quantity": "1480 cases (2 bags per case)",
      "code_info": "F023444",
      "center_classification_date": "20130502",
      "distribution_pattern": "Nationwide Distribution including IL, SC, TX, VA, FL, AR, and NY.",
      "state": "MA",
      "product_description": "NxStage PureFlow-B Solution, Model/Catalog Number: RFP-401, packaged in a case     The NxStage PureFLow-B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.",
      "report_date": "20130508",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "NxStage Medical, Inc.",
      "recall_number": "Z-1214-2013",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "64820",
      "termination_date": "20140917",
      "more_code_info": "",
      "recall_initiation_date": "20130318",
      "postal_code": "01843-1748",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}